Register now! Celebrate the National CMV Foundation’s 10th anniversary by joining us as we walk, run, or roll in the 5th Annual #Strides4CMV Worldwide Virtual 5k happening Saturday, June 29th! 🗓️ Register and check out our training tips here: ow.ly/mNke50RaSlB #StopCMV

The @US_FDA is holding a public, two-day workshop entitled “Development of Drugs for the Treatment of Congenital Cytomegalovirus (CMV) Infection and Neonatal Enterovirus Infection.” Go here to learn more and to register: ow.ly/tVON50RgAKi #StopCMV

Help to continue the fight to #StopCMV by supporting the Stop CMV Act! 🧡 Here's how you can help.⬇️ 🟦Contact your legislators to ask them to co-sponsor The Stop CMV Act. 🟦 Support our advocacy work by donating on our website here: ow.ly/tvBU50RaUKj #CMVAwareness

Big thank you to all the incredible sponsors of Run With Rob 2024! 🏃‍♂️ Your support means the world to us and makes this event possible. We couldn't do it without you! 🙌 #RunWithRob2024 #CommunitySupport #StopCMV

@NationalCMV SAC member, Dr. Angela Shoup, was recently selected to receive the Honors of the American Academy of Audiology (AAA). Read about the award recipients here: ow.ly/KEhP50RjlaJ #StopCMV #AmericanAcademyofAudiology

The Board of Directors for @NationalCMV is recruiting new governing board members. We are seeking applicants who have a passion for the NCMVF mission and vision. Read more about the role and apply here: forms.gle/7G3V52ny1YBaaw… #StopCMV

Our friends at the @nationaldb_ncdb have teamed up with the @chargesyndrome to host 3 webinars that may be useful for families with a child who is deafblind. Check out the website for more info! The webinars will be recorded. ow.ly/G1OC50RgvFm #StopCMV

Register now! Celebrate the National CMV Foundation’s 10th anniversary by joining us as we walk, run, or roll in the 5th Annual #Strides4CMV Worldwide Virtual 5k happening Saturday, June 29th! 🗓️ Register here: strides4cmvww.funraise.org #StopCMV

Help to continue the fight to #StopCMV by supporting the Stop CMV Act! 🧡 Here's how you can help.⬇️ 🟦Contact your legislators to ask them to co-sponsor The Stop CMV Act. 🟦 Support our advocacy work by donating on our website here: ow.ly/tvBU50RaUKj #CMVAwareness

Help the National CMV Foundation commemorate 10 years! We're collecting photos and videos from Foundation events, advocacy efforts, and volunteers. If you have any National CMV photos or videos, please email them to: [email protected] by April 30th. #StopCMV

@TheLancet recently published “Consensus recommendation for prenatal, neonatal and postnatal management of congenital cytomegalovirus infection,” from the European Congenital Infection Initiative. Read the article here: ow.ly/gs2550RjnCK #StopCMV #CMVAwareness

Did you know? It's estimated that about 1 in 200 babies are born with congenital #CMV, making it more common than Down syndrome, fetal alcohol syndrome, or spina bifida. 🤔 Let's work together to change these statistics! 🫶 #CMVAwareness #SpreadTheWord #StopCMV

Thank you to our incredible community for your unwavering support in raising awareness about congenital CMV. Together, we can make a difference! 💙 #Gratitude #StopCMV

Head over to the CMV Canada website and dive into our latest blog! 😎 From breaking news to event announcements, navigating conversations with your kids about CMV, supporting siblings, to early detection in infants - we've got you covered! cmvcanada.com/blog #StopCMV

Help the National CMV Foundation commemorate 10 years! We're collecting photos and videos from Foundation events, advocacy efforts, and volunteers. If you have any National CMV photos or videos please email them to: [email protected] by April 30th. #StopCMV

Did you know that congenital #CMV can lead to long-term health issues like hearing loss and developmental delays? 🤰 Let's raise awareness to support affected families. #StopCMV #AwarenessMatters

This year @NationalCMV is celebrating 10 years of CMV hope and impact. We are excited to share this theme through our annual “Faces of CMV” campaign. We invite you to submit a story to be shared during our celebration. Submit your story here: ow.ly/hb1j50R3s2h #StopCMV

Thanks @thisweekinWoo for sharing our work! @UMassChan @moderna_tx @NationalCMV #worcesterma #StopCMV #CMVawareness

ThisWeekinWorcester @thisweekinWoo

4 weeks ago

Thanks @thisweekinWoo for sharing our work! @UMassChan @moderna_tx @NationalCMV #worcesterma #StopCMV #CMVawareness

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Our friends at @InfantHearing have released a podcast about congenital CMV. This episode features a conversation with CMV advocate, Megan Nix, author of Remedies for Sorrow. Check it out here: ow.ly/tmUm50R7S9U #StopCMV

Meet Patty, Community Alliance Chair & CMV mom! 🧡 Check out the blog and learn why the National CMV Foundation mission is so important to Patty & how she is helping to raise awareness in her home state of Montana. Read the blog here: ow.ly/hrEF50R7IEZ #StopCMV